Shellfish import and hull fouling as vectors for new red algal introductions in the Venice Lagoon

2018 ◽  
Vol 215 ◽  
pp. 30-38 ◽  
Author(s):  
Marion A. Wolf ◽  
Alessandro Buosi ◽  
Abdul-Salam F. Juhmani ◽  
Adriano Sfriso
Keyword(s):  
Author(s):  
Enrico Marchi ◽  
Attilio Adami ◽  
Alfredo Caielli ◽  
Giovanni Cecconi

2018 ◽  
Vol 8 (1) ◽  
pp. 84-99
Author(s):  
Eleonora Sasso

This paper takes as its starting point the conceptual metaphor ‘life is a journey’ as defined by Lakoff and Johnson (1980) in order to advance a new reading of William Michael Rossetti's Democratic Sonnets (1907). These political verses may be defined as cognitive-semantic poems, which attest to the centrality of travel in the creation of literary and artistic meaning. Rossetti's Democratic Sonnets is not only a political manifesto against tyranny and oppression, promoting the struggle for liberalism and democracy as embodied by historical figures such as Napoleon, Mazzini, Cavour, and Garibaldi; but it also reproduces Rossetti's real and imagined journeys throughout Europe in the late nineteenth century. This essay examines these references in light of the issues they raise, especially the poet as a traveller and the journey metaphor in poetry. But its central purpose is to re-read Democratic Sonnets as a cognitive map of Rossetti's mental picture of France and Italy. A cognitive map, first theorised by Edward Tolman in the 1940s, is a very personal representation of the environment that we all experience, serving to navigate unfamiliar territory, give direction, and recall information. In terms of cognitive linguistics, Rossetti is a figure whose path is determined by French and Italian landmarks (Paris, the island of St. Helena, the Alps, the Venice Lagoon, Mount Vesuvius, and so forth), which function as reference points for orientation and are tied to the historical events of the Italian Risorgimento. Through his sonnets, Rossetti attempts to build into his work the kind of poetic revolution and sense of history which may only be achieved through encounters with other cultures.


Our Nature ◽  
2018 ◽  
Vol 16 (1) ◽  
pp. 48-54
Author(s):  
Ram Bhajan Mandal ◽  
Sunila Rai ◽  
Madhav Kumar Shrestha ◽  
Dilip Kumar Jha ◽  
Narayan Prasad Pandit

An experiment was carried to assess the effect of red algal bloom on growth and production of carp, water quality and profit from carp for 120 days at Aquaculture Farm of Agriculture and Forestry University, Chitwan. The experiment included two treatments: carp polyculture in non-red pond and carp polyculture in red pond with algal bloom each with three replicates. Carp fingerlings were stocked at 1 fish/m2 and fed with pellet containing 24% CP at 3% body weight. Net yield of rohu was found significantly higher (p<0.05) in non-red ponds (0.38±0.01 t ha-1) than red ponds (0.24±0.05 t ha-1). Survival of rohu (84.9±1.4%), bighead (95.2±2.0%) and mrigal (88.1±14.4%) were also significantly higher (p<0.05) in non-red ponds than red ponds. Red algal bloom affected DO, nitrate and chlorophyll-a, nitrite, total nitrogen, total phosphorus, total dissolved solids and conductivity. However, overall carp production and profit from carp remained unaffected.


1980 ◽  
Vol 23 (11) ◽  
Author(s):  
Judith L. Connor

AbstractField studies of the benthic macroalgae of fifteen selected Chesapeake Bay oyster communities were conducted over a period of a year (March 1977 to February 1978). Algal distribu tion and seasonal occurrence were studied in relation to changes in the physical environment. Salinity, temperature, and light availability were important factors in the spatial and temporal distributions of algae in these subtidal habitats.Seventeen species of Chlorophyta, Phaeophyta, and Rhodophyta were recorded from the fifteen study sites distributed over 130 kilometers within the Maryland portion of Chesapeake Bay. Species of Chlorophyta were associated with oyster communities throughout the year of study with maximum numbers of species and maximum biomass occurring in spring. Only once was a member of the Phaeophyta encountered; a single filamentous species, Ectocarpus, was collected during winter. Species of Rhodophyta were present throughout the year at the study sites.Most of the algae collected reproduced asexually by spores and/or vegetative fragments. Sexual reproduction occurred in some of the red algal species. The presence of tetrasporic and cystocarpic plants of Dasya baillouviana and Polysiphonia harveyi var. olneyi may indicate that the usual triphasic Florideophycean life history occurs in this estuary.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Harry W. Rathbone ◽  
Katharine A. Michie ◽  
Michael J. Landsberg ◽  
Beverley R. Green ◽  
Paul M. G. Curmi

AbstractPhotosynthetic organisms have developed diverse antennas composed of chromophorylated proteins to increase photon capture. Cryptophyte algae acquired their photosynthetic organelles (plastids) from a red alga by secondary endosymbiosis. Cryptophytes lost the primary red algal antenna, the red algal phycobilisome, replacing it with a unique antenna composed of αβ protomers, where the β subunit originates from the red algal phycobilisome. The origin of the cryptophyte antenna, particularly the unique α subunit, is unknown. Here we show that the cryptophyte antenna evolved from a complex between a red algal scaffolding protein and phycoerythrin β. Published cryo-EM maps for two red algal phycobilisomes contain clusters of unmodelled density homologous to the cryptophyte-αβ protomer. We modelled these densities, identifying a new family of scaffolding proteins related to red algal phycobilisome linker proteins that possess multiple copies of a cryptophyte-α-like domain. These domains bind to, and stabilise, a conserved hydrophobic surface on phycoerythrin β, which is the same binding site for its primary partner in the red algal phycobilisome, phycoerythrin α. We propose that after endosymbiosis these scaffolding proteins outcompeted the primary binding partner of phycoerythrin β, resulting in the demise of the red algal phycobilisome and emergence of the cryptophyte antenna.


2003 ◽  
Vol 107 ◽  
pp. 361-364
Author(s):  
F. de Giorgi ◽  
F. la Marca ◽  
P. Massacci ◽  
E. Vichi

Phytotaxa ◽  
2019 ◽  
Vol 415 (4) ◽  
pp. 233-239
Author(s):  
MARION A. WOLF ◽  
ALESSANDRO BUOSI ◽  
ABDUL-SALAM F. JUHMANI ◽  
ADRIANO SFRISO

Centroceras Kützing is a small red algal genus with 18 currently accepted species (Guiry & Guiry 2019), characterized by simple filamentous thalli with erect axes arising from a prostrate system and di-trichotomous branching (Hommersand 1963). The characters used to distinguish species are primarily cortical filament morphology: shape and number of the acropetal cortical cells, shape of gland cells, and shape of spines (Won et al. 2009). The generitype C. clavulatum (C. Agardh) Montagne has been viewed for a long time as a highly variable and cosmopolitan species (Hommersand 1963). Molecular and detailed morphological analyses brought Barros-Barreto et al. (2006) to report that C. clavulatum may consist of a species complex and Won et al. (2009) confirmed this hypothesis identifying eight taxonomic entities phylogenetically segregated from genuine C. clavulatum. Seven of these entities were assigned to the following species: C. gasparrinii (Meneghini) Kützing, C. hommersandii Won, T.O. Cho & Fredericq, C. hyalacanthum Kützing, C. micracanthum Kützing, C. natalensis Won, T.O. Cho & Fredericq, C. rodmanii Won, T.O. Cho & Fredericq, and C. tetrachotomum Won, T.O. Cho & Fredericq, (Won et al. 2009). Centroceras gasparrinii, C. hyalacanthum, and C. micracanthum are three western Atlantic species listed as synonyms of C. clavulatum since the middle of the 19th century and resurrected from the ‘C. clavulatum complex’ by Won et al. (2009). In particular, two of these taxa were described from specimens of the Mediterranean Sea: C. gasparrinii (as Ceramium gasparrinii Meneghini, type locality Palermo, Italy) and C. micracanthum (reported with the synonym Centroceras leptacanthum Kützing, type locality Genoa, Italy). Therefore, the numerous Mediterranean records of C. clavulatum (e.g., Gómez Garreta et al. 2001; Verlaque 2001; Sfriso & Curiel 2007; Taşkýn et al. 2013) most probably belong to one of these two species and have to be re-examined for a correct identification and to understand the spatial distribution of the different taxa (Tsiamis et al. 2010). For this reason, in the last years in Greece (Tsiamis et al. 2010), Spain (Gallardo et al. 2016) and Morocco (Hassoun et al. 2018) accurate sampling and morphological analyses of specimens previously identified as C. clavulatum were conducted to determine their correct taxonomic identities. In all cases the recognized species was C. gasparrinii, which can be distinguished morphologically from the other ones previously known as C. clavulatum by the presence of ovoid gland cells and ovoid terminal acropetal cortical cells (Won et al. 2009). As reported by Tsiamis et al. (2010), Greek samples differed from those described by Won et al. (2009), in the smaller number of periaxial cells (10–12 against 13–19).


2020 ◽  
Vol 28 (6) ◽  
pp. 28-35
Author(s):  
Julia Van Etten
Keyword(s):  


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